Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
InVision-Plus and InVision-Plus Junior Needleless IV Connector Recalled by Rymed Technologies, LLC Due to Potential for the female luer component of the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Rymed Technologies, LLC directly.
Affected Products
InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.
Quantity: 496,400 units
Why Was This Recalled?
Potential for the female luer component of the InVision-Plus IV connector to crack during use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Rymed Technologies, LLC
Rymed Technologies, LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report